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Polysite 2000 Con Introduttore - 5F

by Vygon Italia SRL

Ref A201501B

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805960273D01A2015-1CBG Basic UDI-DI 08059602733924UDI-DIDate22 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
A201501B
Primary DI / UDI-DI
08059602733924
Basic UDI-DI
805960273D01A2015-1CBG
EMDN Code
C01020401 Subcutaneous implantable venous access port systems, single-chamber
Device Class
Class III
Medical Purpose
Kit per l’impianto di un CVC con camera impiantabile con introduttore a guaina apribile

Manufacturer details

EUDAMED SRN
IT-PR-000012626

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Properties

Other properties (1)

  • Sterile: No